# Olopatadine Hydrochloride

NDC: 46708-710
Generic name: olopatadine hydrochloride
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION/ DROPS
Routes: OPHTHALMIC
Marketing started: 20210125

FDA application: ANDA209420

## Active ingredients

- OLOPATADINE HYDROCHLORIDE: 2 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46708-710"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-710
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ba550d08-a2de-45e7-b053-6bbecdff138b